PE20010629A1 - TRIAZOLPYRIDINAMINE DERIVATIVES AS ADENOSINE RECEPTOR LINKS - Google Patents
TRIAZOLPYRIDINAMINE DERIVATIVES AS ADENOSINE RECEPTOR LINKSInfo
- Publication number
- PE20010629A1 PE20010629A1 PE2000000903A PE0009032000A PE20010629A1 PE 20010629 A1 PE20010629 A1 PE 20010629A1 PE 2000000903 A PE2000000903 A PE 2000000903A PE 0009032000 A PE0009032000 A PE 0009032000A PE 20010629 A1 PE20010629 A1 PE 20010629A1
- Authority
- PE
- Peru
- Prior art keywords
- pyridin
- phenyl
- derivatives
- ilamine
- triazol
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/16—Central respiratory analeptics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Pulmonology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Immunology (AREA)
- Psychology (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Addiction (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Anesthesiology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
SE REFIERE A DERIVADOS DE AMINO-TRIAZOLPIRIDINA DE FORMULA I, DONDE R1 ES HETEROARILO DE 5-6 MIEMBROS, (CH2)nOH, O(CH2)nFENILO, BENZOFURILO, INDOLILO, BENZOTIOFENILO, S-ALQUILO; R2 Y R4 SON H, CIANO, S(O)2-FENILO; R3 ES H, HALOGENO, HETEROARILO 5-6 MIEMBROS, FENILO, O-FENILO, ENTRE OTROS; R5 ES NR2, R2 ES H, ALQUILO, FENILO, BENCILO, ALQUILO, CO-ALCOXI, ALQUENILO, CO(CH2)nFENILO, ENTRE OTROS; n ES 0-4. SON COMPUESTOS PREFERIDOS 2-FURAN-2-IL-7-PIRIDIN-4-IL-[1,2,4]TRIAZOL[1,5-a]PIRIDIN-5-ILAMINA, 2-FURAN-2-IL-7-PIRIDIN-3-IL-[1,2,4]TRIAZOL[1,5-a]PIRIDIN-5-ILAMINA, 2-FURAN-2-IL-7-PIRIDIN-2-IL-[1,2,4]TRIAZOL[1,5-a]PIRIDIN-5-ILAMINA, 7-(4-CLORO-FENIL)-2-(5-METIL-FURAN-2-IL)-[1,2,4]TRIAZOL[1,5-a]PIRIDIN-5-ILAMINA, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO PARA LA PREPARACION. LOS DERIVADOS DE AMINO-TRIAZOLPIRIDINA SON LIGANDOS RECEPTORES DE ADENOSINA Y PUEDEN SER UTILES EN LA REGULACION DEL METABOLISMO CELULAR, MODULACION DE ACTIVIDADES DEL SISTEMA NERVIOSO CENTRAL Y ENFERMEDADES COMO ALZHEIMER, PARKINSON, ESQUIZOFRENIAREFERS TO AMINO-TRIAZOLPYRIDINE DERIVATIVES OF FORMULA I, WHERE R1 IS 5-6 MEMBER HETEROARYL, (CH2) nOH, OR (CH2) nPHENYL, BENZOFURIL, INDOLYL, BENZOTHYL, S-ALKYL; R2 AND R4 ARE H, CYANE, S (O) 2-PHENYL; R3 IS H, HALOGEN, HETEROARYL 5-6 MEMBERS, PHENYL, O-PHENYL, AMONG OTHERS; R5 IS NR2, R2 IS H, ALKYL, PHENYL, BENZYL, ALKYL, CO-ALCOXY, ALKENYL, CO (CH2) nPHENYL, AMONG OTHERS; n IS 0-4. PREFERRED COMPOUNDS ARE 2-FURAN-2-IL-7-PYRIDIN-4-IL- [1,2,4] TRIAZOL [1,5-a] PYRIDIN-5-ILAMINE, 2-FURAN-2-IL-7- PYRIDIN-3-IL- [1,2,4] TRIAZOL [1,5-a] PYRIDIN-5-ILAMINE, 2-FURAN-2-IL-7-PYRIDIN-2-IL- [1,2,4] TRIAZOL [1,5-a] PYRIDIN-5-ILAMINE, 7- (4-CHLORO-PHENYL) -2- (5-METHYL-FURAN-2-IL) - [1,2,4] TRIAZOL [1,5 -a] PYRIDIN-5-ILAMINE, AMONG OTHERS. IT ALSO REFERS TO A PROCEDURE FOR PREPARATION. AMINO-TRIAZOLPYRIDINE DERIVATIVES ARE ADENOSINE RECEPTORS AND MAY BE USEFUL IN THE REGULATION OF CELLULAR METABOLISM, MODULATION OF CENTRAL NERVOUS SYSTEM ACTIVITIES AND DISEASES SUCH AS ALZHEIMER, PARKINSONIA, SCHIZOFRENIA
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP99117578 | 1999-09-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20010629A1 true PE20010629A1 (en) | 2001-05-30 |
Family
ID=8238933
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2000000903A PE20010629A1 (en) | 1999-09-06 | 2000-09-04 | TRIAZOLPYRIDINAMINE DERIVATIVES AS ADENOSINE RECEPTOR LINKS |
Country Status (22)
Country | Link |
---|---|
US (1) | US6355653B1 (en) |
EP (1) | EP1214322A2 (en) |
JP (1) | JP2003528811A (en) |
KR (1) | KR20020027625A (en) |
CN (1) | CN1379777A (en) |
AR (1) | AR037484A1 (en) |
AU (1) | AU7511000A (en) |
BR (1) | BR0013792A (en) |
CA (1) | CA2383998A1 (en) |
CZ (1) | CZ20021220A3 (en) |
HR (1) | HRP20020172A2 (en) |
HU (1) | HUP0203316A3 (en) |
IL (1) | IL148167A0 (en) |
MA (1) | MA26816A1 (en) |
MX (1) | MXPA02001748A (en) |
NO (1) | NO20021077L (en) |
PE (1) | PE20010629A1 (en) |
PL (1) | PL354240A1 (en) |
TR (1) | TR200200579T2 (en) |
WO (1) | WO2001017999A2 (en) |
YU (1) | YU13502A (en) |
ZA (1) | ZA200201055B (en) |
Families Citing this family (49)
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US6506772B1 (en) * | 2000-12-15 | 2003-01-14 | Hoffmann-La Roche Inc. | Substituted [1,2,4]triazolo[1,5a]pyridine derivatives with activity as adenosine receptor ligands |
US6514989B1 (en) | 2001-07-20 | 2003-02-04 | Hoffmann-La Roche Inc. | Aromatic and heteroaromatic substituted 1,2,4-triazolo pyridine derivatives |
RU2296763C2 (en) * | 2001-10-08 | 2007-04-10 | Ф.Хоффманн-Ля Рош Аг | 8-amino-[1,2,4]triazolo-[1,5-a]pyridine-6-carboxylic acid amide and medicinal agent comprising thereof |
US6693116B2 (en) * | 2001-10-08 | 2004-02-17 | Hoffmann-La Roche Inc. | Adenosine receptor ligands |
IL161573A0 (en) | 2001-11-30 | 2004-09-27 | Schering Corp | [1,2,4]-TRIAZOLE BICYCLIC ADENOSINE A2a RECEPTOR ANTAGONISTS |
HUP0105407A3 (en) * | 2001-12-21 | 2004-04-28 | Sanofi Aventis | Triazolo[1,5-a]quinolin derivatives, process for their preparation, pharmaceutical compositions thereof and intermediates |
WO2003063876A2 (en) | 2002-01-28 | 2003-08-07 | Kyowa Hakko Kogyo Co., Ltd. | Methods of treating patients suffering from movement disorders |
CA2489252A1 (en) * | 2002-06-13 | 2003-12-24 | Pfizer Inc. | Non-peptide gnrh agents, pharmaceutical compositions and methods for their use |
EP1711498A2 (en) * | 2004-01-26 | 2006-10-18 | Altana Pharma AG | 1,2,4-triazolo¬1,5-a|pyridines as gastric acid secretion inhibitors |
JP2008524330A (en) | 2004-12-21 | 2008-07-10 | シェーリング コーポレイション | Pyrazolo [1,5-A] pyrimidine adenosine A2a receptor antagonist |
ES2273599B1 (en) | 2005-10-14 | 2008-06-01 | Universidad De Barcelona | COMPOUNDS FOR THE TREATMENT OF HEADPHONE FIBRILATION. |
WO2008014199A2 (en) * | 2006-07-28 | 2008-01-31 | Boehringer Ingelheim International Gmbh | Sulfonyl compounds which modulate the cb2 receptor |
EP2074084B1 (en) * | 2006-09-25 | 2013-08-28 | Boehringer Ingelheim International GmbH | Compounds which modulate the cb2 receptor |
EP2096923B1 (en) * | 2006-11-27 | 2014-01-22 | H. Lundbeck A/S | Heteroaryl amide derivatives |
JP2010511018A (en) * | 2006-12-01 | 2010-04-08 | ガラパゴス・ナムローゼ・フェンノートシャップ | Triazolopyridine compounds useful for the treatment of degenerative and inflammatory diseases |
UA99610C2 (en) * | 2007-04-10 | 2012-09-10 | Х. Луннбэк А/С | Heteroaryl amide analogues as p2x7 antagonists |
WO2009017954A1 (en) * | 2007-08-01 | 2009-02-05 | Phenomix Corporation | Inhibitors of jak2 kinase |
GB0719803D0 (en) | 2007-10-10 | 2007-11-21 | Cancer Rec Tech Ltd | Therapeutic compounds and their use |
CA2704684A1 (en) * | 2007-11-07 | 2009-05-14 | Boehringer Ingelheim International Gmbh | Compounds which modulate the cb2 receptor |
US20120015988A1 (en) * | 2008-05-13 | 2012-01-19 | Boehringer Ingelheim International Gmbh | Sulfone Compounds Which Modulate The CB2 Receptor |
PE20110063A1 (en) * | 2008-06-20 | 2011-02-16 | Genentech Inc | DERIVATIVES OF [1, 2, 4] TRIAZOLO [1, 5-a] PYRIDINE AS JAK INHIBITORS |
CN102131389A (en) * | 2008-06-20 | 2011-07-20 | 健泰科生物技术公司 | Triazolopyridine JAK inhibitor compounds and methods |
WO2010005782A1 (en) * | 2008-07-10 | 2010-01-14 | Boehringer Ingelheim International Gmbh | Sulfone compounds which modulate the cb2 receptor |
TWI453207B (en) * | 2008-09-08 | 2014-09-21 | Signal Pharm Llc | Aminotriazolopyridines, compositions thereof, and methods of treatment therewith |
CN102164917A (en) * | 2008-09-25 | 2011-08-24 | 贝林格尔.英格海姆国际有限公司 | Compounds which selectively modulate the CB2 receptor |
MY153913A (en) * | 2009-05-12 | 2015-04-15 | Janssen Pharmaceuticals Inc | 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
EP2438066A2 (en) | 2009-06-05 | 2012-04-11 | Cephalon, Inc. | PREPARATION AND USES OF 1,2,4-TRIAZOLO [1,5a]PYRIDINE DERIVATIVES |
US8299103B2 (en) * | 2009-06-15 | 2012-10-30 | Boehringer Ingelheim International Gmbh | Compounds which selectively modulate the CB2 receptor |
JP5756800B2 (en) | 2009-06-16 | 2015-07-29 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Azetidine 2-carboxamide derivative that modulates CB2 receptor |
EP2746282A1 (en) * | 2009-07-17 | 2014-06-25 | Japan Tobacco Inc. | Triazolopyridine compound, and action thereof as prolyl hydroxylase inhibitor and erythropoietin production inducer |
JP2013505295A (en) * | 2009-09-22 | 2013-02-14 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Compound that selectively modulates CB2 receptor |
US9315454B2 (en) | 2010-01-15 | 2016-04-19 | Boehringer Ingelheim International Gmbh | Compounds which modulate the CB2 receptor |
EP2542539B1 (en) | 2010-03-05 | 2014-02-26 | Boehringer Ingelheim International GmbH | Tetrazole compounds which selectively modulate the cb2 receptor |
JP5746764B2 (en) | 2010-07-22 | 2015-07-08 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Compounds that modulate the CB2 receptor |
EP2758396B1 (en) * | 2011-09-19 | 2017-03-29 | F. Hoffmann-La Roche AG | Triazolopyridine compounds as pde10a inhibitors |
WO2013043518A1 (en) | 2011-09-22 | 2013-03-28 | Merck Sharp & Dohme Corp. | Imidazopyridyl compounds as aldosterone synthase inhibitors |
US9193724B2 (en) | 2011-09-22 | 2015-11-24 | Merck Sharp & Dohme Corp. | Triazolopyridyl compounds as aldosterone synthase inhibitors |
EP2803668A1 (en) | 2013-05-17 | 2014-11-19 | Boehringer Ingelheim International Gmbh | Novel (cyano-dimethyl-methyl)-isoxazoles and -[1,3,4]thiadiazoles |
TW201808906A (en) | 2016-03-16 | 2018-03-16 | 拜耳作物科學股份有限公司 | Substituted pyridine compounds as pesticides |
CN106543175B (en) * | 2016-10-28 | 2018-06-01 | 上海大学 | Triaryl [1,2,4] triazole [1,5-a] pyridine derivate and preparation method thereof |
JP7111733B2 (en) * | 2017-03-16 | 2022-08-02 | 江蘇恒瑞医薬股▲ふん▼有限公司 | Heteroaryl[4,3-c]pyrimidin-5-amine derivatives, methods for their preparation, and pharmaceutical uses thereof |
MA52422A (en) | 2018-02-27 | 2021-01-06 | Incyte Corp | IMIDAZOPYRIMIDINES AND TRIAZOLOPYRIMIDINES AS A2A / A2B INHIBITORS |
JP7391046B2 (en) | 2018-05-18 | 2023-12-04 | インサイト・コーポレイション | Fused pyrimidine derivatives as A2A/A2B inhibitors |
CN117304191A (en) | 2018-07-05 | 2023-12-29 | 因赛特公司 | Fused pyrazine derivatives as A2A/A2B inhibitors |
JP7399589B2 (en) * | 2018-09-12 | 2023-12-18 | 日本化薬株式会社 | pest control agent |
CN114787160B (en) | 2018-12-20 | 2025-03-25 | 因赛特公司 | Imidazopyridazines and imidazopyridines as inhibitors of activin receptor-like kinase-2 |
TWI829857B (en) | 2019-01-29 | 2024-01-21 | 美商英塞特公司 | Pyrazolopyridines and triazolopyridines as a2a / a2b inhibitors |
AU2022206418A1 (en) * | 2021-01-09 | 2022-10-13 | Bugworks Research, Inc. | Diaminopyrazolo[1,5-a]pyrimidine-6-carbonitrile compounds as adenosine 2a receptor and adenosine 2b receptor antagonist |
CN116082335A (en) * | 2023-01-16 | 2023-05-09 | 上海凌凯医药科技有限公司 | A kind of preparation method of diaryl ether compound |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9226735D0 (en) | 1992-12-22 | 1993-02-17 | Ici Plc | Azole derivatives |
WO1999043678A1 (en) | 1998-02-24 | 1999-09-02 | Kyowa Hakko Kogyo Co., Ltd. | Remedies/preventives for parkinson's disease |
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2000
- 2000-08-24 US US09/645,127 patent/US6355653B1/en not_active Expired - Fee Related
- 2000-08-28 AU AU75110/00A patent/AU7511000A/en not_active Abandoned
- 2000-08-28 CZ CZ20021220A patent/CZ20021220A3/en unknown
- 2000-08-28 EP EP00964043A patent/EP1214322A2/en not_active Withdrawn
- 2000-08-28 MX MXPA02001748A patent/MXPA02001748A/en unknown
- 2000-08-28 IL IL14816700A patent/IL148167A0/en unknown
- 2000-08-28 CN CN00812501A patent/CN1379777A/en active Pending
- 2000-08-28 PL PL00354240A patent/PL354240A1/en not_active Application Discontinuation
- 2000-08-28 TR TR2002/00579T patent/TR200200579T2/en unknown
- 2000-08-28 HU HU0203316A patent/HUP0203316A3/en unknown
- 2000-08-28 JP JP2001522222A patent/JP2003528811A/en active Pending
- 2000-08-28 BR BR0013792-8A patent/BR0013792A/en not_active IP Right Cessation
- 2000-08-28 YU YU13502A patent/YU13502A/en unknown
- 2000-08-28 KR KR1020027002990A patent/KR20020027625A/en not_active Application Discontinuation
- 2000-08-28 WO PCT/EP2000/008372 patent/WO2001017999A2/en not_active Application Discontinuation
- 2000-08-28 CA CA002383998A patent/CA2383998A1/en not_active Abandoned
- 2000-09-04 AR ARP000104612A patent/AR037484A1/en not_active Application Discontinuation
- 2000-09-04 PE PE2000000903A patent/PE20010629A1/en not_active Application Discontinuation
-
2002
- 2002-02-06 ZA ZA200201055A patent/ZA200201055B/en unknown
- 2002-02-26 HR HR20020172A patent/HRP20020172A2/en not_active Application Discontinuation
- 2002-03-05 NO NO20021077A patent/NO20021077L/en not_active Application Discontinuation
- 2002-03-06 MA MA26540A patent/MA26816A1/en unknown
Also Published As
Publication number | Publication date |
---|---|
US6355653B1 (en) | 2002-03-12 |
IL148167A0 (en) | 2002-09-12 |
WO2001017999A3 (en) | 2001-12-06 |
CZ20021220A3 (en) | 2002-10-16 |
BR0013792A (en) | 2002-05-14 |
AU7511000A (en) | 2001-04-10 |
JP2003528811A (en) | 2003-09-30 |
HUP0203316A3 (en) | 2004-07-28 |
ZA200201055B (en) | 2003-07-30 |
MXPA02001748A (en) | 2002-08-06 |
NO20021077D0 (en) | 2002-03-05 |
KR20020027625A (en) | 2002-04-13 |
EP1214322A2 (en) | 2002-06-19 |
TR200200579T2 (en) | 2002-12-23 |
HUP0203316A2 (en) | 2003-01-28 |
MA26816A1 (en) | 2004-12-20 |
NO20021077L (en) | 2002-03-05 |
CA2383998A1 (en) | 2001-03-15 |
HRP20020172A2 (en) | 2003-10-31 |
AR037484A1 (en) | 2004-11-17 |
YU13502A (en) | 2004-11-25 |
PL354240A1 (en) | 2003-12-29 |
WO2001017999A2 (en) | 2001-03-15 |
CN1379777A (en) | 2002-11-13 |
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